Nordvall Gunnar, Lundkvist Johan, Sandin Johan
AlzeCure Pharma AB, Huddinge, Sweden.
Department of Neurobiology, Care Sciences, and Society, Division of Neurogeriatrics, Center for Alzheimer Research, Karolinska Institutet, Stockholm, Sweden.
Front Mol Neurosci. 2023 Oct 16;16:1279740. doi: 10.3389/fnmol.2023.1279740. eCollection 2023.
Recent clinical data with three therapeutic anti-Aβ antibodies have demonstrated that removal of Aβ-amyloid plaques in early Alzheimer's disease (AD) can attenuate disease progression. This ground-breaking progress in AD medicine has validated both the amyloid cascade hypothesis and Aβ-amyloid as therapeutic targets. These results also strongly support therapeutic approaches that aim to reduce the production of amyloidogenic Aβ to prevent the formation of Aβ-pathology. One such strategy, so-called gamma-secretase modulators (GSM), has been thoroughly explored in preclinical settings but has yet to be fully tested in clinical trials. Recent scientific progress has shed new light on the role of Aβ in Alzheimer's disease and suggests that GSMs exhibit specific pharmacological features that hold great promise for the prevention and treatment of Alzheimer's disease. In this short review, we discuss the data that support why it is important to continue to progress in this class of compounds.
最近三种治疗性抗Aβ抗体的临床数据表明,在早期阿尔茨海默病(AD)中清除Aβ淀粉样斑块可以减缓疾病进展。AD医学领域的这一突破性进展证实了淀粉样蛋白级联假说以及Aβ淀粉样蛋白作为治疗靶点的有效性。这些结果也有力地支持了旨在减少淀粉样Aβ生成以预防Aβ病理形成的治疗方法。一种这样的策略,即所谓的γ-分泌酶调节剂(GSM),已在临床前研究中得到充分探索,但尚未在临床试验中进行全面测试。最近的科学进展为Aβ在阿尔茨海默病中的作用带来了新的认识,并表明GSM具有特定的药理学特性,对阿尔茨海默病的预防和治疗具有巨大潜力。在这篇简短的综述中,我们讨论了支持这类化合物为何有必要继续推进研究的数据。